285-IF) using Mouse Anti-Human Indoleamine 2,3-dioxygenase/IDO Monoclonal Antibody (Catalog # MAB6030) at 10 µg/mL for 3 hours at room temperature. Cells were stained using the NorthernLights™ 557-conjugated Anti-Mouse IgG Secondary Antibody (red; Catalog #
NL007) and counter-stained with DAPI (blue). Specific staining was localized to cytoplasm. View our protocol for
Fluorescent ICC Staining of Cells on Coverslips." class="big_lightbox">

285-IF) using Mouse Anti-Human Indoleamine 2,3-dioxygenase/IDO Monoclonal Antibody (Catalog # MAB6030) at 10 µg/mL for 3 hours at room temperature. Cells were stained using the NorthernLights™ 557-conjugated Anti-Mouse IgG Secondary Antibody (red; Catalog #
NL007) and counter-stained with DAPI (blue). Specific staining was localized to cytoplasm. View our protocol for
Fluorescent ICC Staining of Cells on Coverslips." alt="Indoleamine 2,3-dioxygenase/IDO was detected in immersion fixed A431 human epithelial carcinoma cells stimulated with 0.5 ng/mL of Recombinant Human IFN-gamma (Catalog #
285-IF) using Mouse Anti-Human Indoleamine 2,3-dioxygenase/IDO Monoclonal Antibody (Catalog # MAB6030) at 10 µg/mL for 3 hours at room temperature. Cells were stained using the NorthernLights™ 557-conjugated Anti-Mouse IgG Secondary Antibody (red; Catalog #
NL007) and counter-stained with DAPI (blue). Specific staining was localized to cytoplasm. View our protocol for
Fluorescent ICC Staining of Cells on Coverslips." class="big_thumb" />
206-IL) and 10 ng/mL Recombinant Human GM-CSF (Catalog #
215-GM) for 7 days were stained with Mouse Anti-Human Siglec-3/CD33 APC-conjugated Monoclonal Antibody (Catalog #
FAB1137A) and either (A) Mouse Anti-Human Indoleamine 2,3-dioxygenase/IDO Monoclonal Antibody (Catalog # MAB6030) or (B) Mouse IgG
1Isotype Control (Catalog #
MAB002) followed by Phycoerythrin-conjugated Anti-Mouse IgG Secondary Antibody (Catalog #
F0102B). To facilitate intracellular staining, cells were fixed with paraformaldehyde and permeabilized with saponin. View our protocol for
Staining Intracellular Molecules." class="big_lightbox">

206-IL) and 10 ng/mL Recombinant Human GM-CSF (Catalog #
215-GM) for 7 days were stained with Mouse Anti-Human Siglec-3/CD33 APC-conjugated Monoclonal Antibody (Catalog #
FAB1137A) and either (A) Mouse Anti-Human Indoleamine 2,3-dioxygenase/IDO Monoclonal Antibody (Catalog # MAB6030) or (B) Mouse IgG
1Isotype Control (Catalog #
MAB002) followed by Phycoerythrin-conjugated Anti-Mouse IgG Secondary Antibody (Catalog #
F0102B). To facilitate intracellular staining, cells were fixed with paraformaldehyde and permeabilized with saponin. View our protocol for
Staining Intracellular Molecules." class="big_thumb" />
MAGH105) and cultured overnight with (A) 50 ng/mL Recombinant Human MCSF (Catalog #
216-MC), 50 ng/mL Recombinant Human IFNg (Catalog #
285-IF) and 50 ng/mL LPS, or (B) Recombinant Human MCSF alone. Cells were stained with Mouse Anti-Human Indoleamine 2,3-dioxygenase/IDO Monoclonal Antibody (Catalog # MAB6030) followed by APC-conjugated Anti-Mouse IgG Secondary Antibody (Catalog #
F0101B) and Mouse Anti-Human CD14 PE-conjugated Monoclonal Antibody (Catalog #
FAB3832P). Quadrant markers were set based on Mouse IgG1 Isotype Control (Catalog #
MAB002). To facilitate intracellular staining, cells were fixed with 1% paraformaldehyde and permeabilized with saponin. View our protocol for
Staining Intracellular Molecules." class="big_lightbox">

MAGH105) and cultured overnight with (A) 50 ng/mL Recombinant Human MCSF (Catalog #
216-MC), 50 ng/mL Recombinant Human IFNg (Catalog #
285-IF) and 50 ng/mL LPS, or (B) Recombinant Human MCSF alone. Cells were stained with Mouse Anti-Human Indoleamine 2,3-dioxygenase/IDO Monoclonal Antibody (Catalog # MAB6030) followed by APC-conjugated Anti-Mouse IgG Secondary Antibody (Catalog #
F0101B) and Mouse Anti-Human CD14 PE-conjugated Monoclonal Antibody (Catalog #
FAB3832P). Quadrant markers were set based on Mouse IgG1 Isotype Control (Catalog #
MAB002). To facilitate intracellular staining, cells were fixed with 1% paraformaldehyde and permeabilized with saponin. View our protocol for
Staining Intracellular Molecules." class="big_thumb" />